|| List of recent Electrophoresis-related patents
| Plasmid-encoded neurotoxin genes in clostridium botulinum serotype a subtypes|
The present invention provides a novel isolated plasmid, wherein the plasmid is a native plasmid found in unique c. Botulinum type a strains and encode either bont/a3 or bont/a4 and bont/b.
| Methods and devices for multi-color, out-of-phase detection in electrophoresis|
The disclosure provides methods and devices for separating and detecting nucleic acid fragments labeled with a plurality of spectrally resolvable dyes using a single light source or multiple light sources. Use of a greater number of light sources increases the number of spectrally resolvable dyes that can be interrogated.
| Expanding cam lock for sealing slab gels in an electrophoresis apparatus|
An expanding cam lock for use with an electrophoresis system is disclosed herein. The cam lock allows the simultaneous use of multiple slab gel cassettes in first and second buffer core assemblies in an electrophoresis system while maintaining the necessary compressive force to create a liquid-tight seal between the anode and cathode buffer solutions.
| System for rapid high-resolution gel electrophoresis|
Electrophoretic systems, formulations and methods are described which allow a user to perform electrophoresis experiments under conditions of high voltage and with reduced run time. An electrophoretic system, formulation or method may be run at 50% higher field strength than comparable systems already in use in the art.
| Microfluidics with wirelessly powered electronic circuits|
Techniques, devices and systems are described for incorporating a printed circuit with a microfluidic device and wirelessly powering the microfluidic device. In one aspect, a microfluidic device includes a substrate with a fluidic channel to provide a path for a fluid with particles.
|Two-dimensional gel electrophoresis apparatus and method|
Two-dimensional gel electrophoresis apparatus includes an electrophoresis zone having four edges defined by a plurality of electrodes. A pair of opposed edges are defined by groups of discrete electrodes.
|High-throughput multi laser wave mixing detection methods and apparatus|
This invention relates to methods and apparatus of a combination of multi-laser wave mixing technology with diagnostic flow technologies with embodiments describing capillary electrophoresis. The unique combination of these technologies along with minute detection levels not yet been seen in the field..
|High-throughput single laser wave mixing detection methods and apparatus|
This invention relates to methods and apparatus of a combination of a single laser wave mixing technology with a diagnostic flow technologies with embodiments describing capillary electrophoresis. The unique combination of these technologies along with minute detection levels not yet been seen in the field..
|Ex-vivo multi-dimensional system for the separation and isolation of cells, vesicles, nanoparticles, and biomarkers|
Devices and techniques are described that involve a combination of multidimensional electrokinetic, dielectrophoretic, electrophoretic and fluidic forces and effects for separating cells, nanovesicles, nanoparticulates and biomarkers (dna, rna, antibodies, proteins) in high conductance (ionic) strength biological samples and buffers. In disclosed embodiments, a combination of continuous and/or pulsed dielectrophoretic (dep) forces, continuous and/or pulsed field dc electrophoretic forces, microelectrophoresis and controlled fluidics are utilized with arrays of electrodes.
|Modified electrode buffers for stain-free protein detection in electrophoresis|
Proteins that are electrophoretically separated in a gel are derivatized to produce fluorescent emissions by incorporating halo-substituted organic compounds into one or both of the electrode buffer solutions at the two ends of the gel. The halo-substituted compounds used are ones that bear an electric charge at the ph of the buffer solutions and gel, and the polarity of the charge on the compounds is such that the compounds migrate from the electrode buffer into the gel under the electrophoretic influence concurrently with the migration of the proteins into the gel.
A particle transporter based on travelling-wave dielectrophoresis is provided. The particle transporter includes a first collection electrode and a second collection electrode on a substrate.
A particle transporter based on travelling-wave dielectrophoresis is provided. The particle transporter includes a common electrode, a plurality of left switch electrodes and a plurality of right switch electrodes.
|Capillary tubes for electrophoresis|
The present invention relates to a plastic capillary tube for capillary electrophoresis, in which the plastic capillary tube has an inlet opening and an outlet opening and, furthermore, has at least one hole in the capillary tube wall and the diameter of the hole on the inside of the capillary tube wall dl(innen) lies in the range from 0.5 μm to 30 μm.. .
|Method of electrophoresing nucleic acids, method of concentrating and purifying nucleic acids, cartridge for nucleic acid electrophoresis, and method of producing cartridge for nucleic acid electrophoresis|
[solving means] a method of electrophoresis includes electrophoresing a nucleic acid in which an intercalator having an anionic functional group has been inserted. The method includes mixing a sample containing a nucleic acid, a compound having a functional group which undergoes dehydration condensation reaction with carboxyl groups included in substances contained in the sample and a condensing agent of dehydration condensation reaction; and electrophoresing the nucleic acid.
|Method for detecting biomolecules using a capacitive touch screen|
A method of detecting biomolecule according to the present invention uses a capacitive touch screen capable of being cheaply manufactured on a large scale, such that the method may have advantages such as cheap cost and a short analysis time and simply detect biomolecules in a personal terminal such as a smart phone, a tablet pc, and the like, on which a capacitive touch screen is mounted, as compared to the existing method requiring an expensive exclusive analysis apparatus based on absorbance or fluorescence having a large volume, a skilled experimental technique such as electrophoresis, or a long analysis time to thereby be performed only in an experimental room equipped with specialists and equipment.. .
|Reduced artifact denaturing capillary electrophoresis of nucleic acids|
Described are methods of reducing the incidence and/or magnitude of artifacts in denaturing nucleic acid capillary electrophoresis (ce). Methods and systems described serve to dismiss non-denatured dna from the tip of the capillary after sample injection and prior to electrophoretic separation of loaded nucleic acids.
|Method for making cu2-xse nanoparticles and method for making deposited cu2-xse thin film by electrophoresis|
In the present invention, copper(i) selenide (cu2-xse) nanoparticles are fabricated by pyrolysis in an inert atmosphere. Uniformly dispersed cu2-xse particles are synthesized by altering cu/se ratio, the concentration of se precursors (top se), reaction time and temperature.
|Electrophoretic material, electrophoresis display device, and electronic apparatus|
In an electrophoretic material, first particles which are charged with a first polarity and second particles which are charged with a second polarity are dispersed in a solvent. A volume, which is obtained by dividing a volume of the solvent by a total number of particles, is called free volume, and a radius of a spherical space, which is occupied by sum of an average volume of the particles and the free volume, is called a free volume radius.
|Aqueous transfer buffer|
The present invention relates to an aqueous transfer buffer that provides superior efficiency in transferring polypeptides of a broad range of molecular weight from a matrix used in electrophoresis to another immobilized surface. Also disclosed are electrophoretic methods and devices in which the aqueous transfer solution of this invention is used..
|Axial illumination for capillary electrophoresis|
System and method for fluorescent light excitation and detection from samples to enhance the numerical aperture and/or reduce the cross-talk of the fluorescent light.. .
|Method for producing a semiconductor chip emitting radiation, semiconductor chip emitting radiation, and component emitting radiation|
A method is provided for producing a radiation-emitting semiconductor chip, in which a first wavelength-converting layer is applied over the radiation exit face of a semiconductor body. The application method is selected from the following group: sedimentation, electrophoresis.
|Optically-induced dielectrophoresis device|
An optically-induced dielectrophoresis device includes a first substrate, a first conductive layer, a first patterned photoconductor layer, a first patterned layer, a second substrate, a second conductive layer, and a spacer. The first conductive layer is disposed on the first substrate.
|Method and microsystem for detecting analytes which are present in drops of liquid|
A detection method of detecting analytes of interest which are present in a liquid. The detection method including the steps of forming drops of liquid on a first surface by capillary breaking of a finger of liquid, which is initially formed by liquid dielectrophoresis.
|Lensed optical fiber for illuminating capillary tube|
An optical fiber (500) illuminates the bore (520) of a capillary tube (515) that is used for separating chemicals by capillary electrophoresis (ce). The fiber terminates in either two sloped regions (525) and a curved region (530) or two sloped regions (705) and a flat region (700).
|Electrophoresis device and display|
An electrophoresis device includes: a plurality of electrophoretic particles included in insulating liquid and configured of a first particle and a second particle, in which the first particle and the second particle have respective charging characteristics that are different from each other; and a porous layer included in the insulating liquid and formed of a fibrous structure.. .
|Analysis of microbes from microcolonies by maldi mass spectrometry|
The invention relates to the cell disruption of microbes and the preparation of the microbe proteins for mass spectrometric analysis. The cells of microbes from microcolonies are disrupted by physical or chemical means directly on the nutrient medium.
|Electrophoresis device and display unit|
There are provided an electrophoresis device and a display unit which are capable of realizing high contrast. The electrophoresis device includes a plurality of electrophoretic particles and a porous layer that are contained in an insulating liquid, the porous layer being formed using a fibrous structure including a plurality of non-migrating particles.
|Main body of electrophoresis device having glass gel cell fast assemble structure|
A electrophoresis device having glass gel cell fast assemble structure is provided, including a main body, a pair of electrode connection terminals attached to the main body, and side clamping parts pivotally connected to the main body on respective side of the main body for maintaining at least one glass gel cell to a surface of the main body. At least one sealing and positioning structure is provided on a surface of the main body including a u-shaped sealing strip partially inlayed on at least one surface of the main body, and at least a pair of positioning poles perpendicularly attached to the main body, wherein the u-shaped sealing strip having a u-shaped body to form a seal between the main body and the gel cell, and positioning protrusions formed on the respective free end of the u-shaped body..
|Multi-color detection system for multiplexed capillary electrophoresis|
A multi-wavelength detector for a multiplex capillary electrophoresis system comprising a linear filter placed in between the capillary detection windows and a 2-dimensional detector. The linear filter is oriented such that the change in wavelength of the filter is in the direction of flow of the fluid within the capillary detection windows.
|Expulsion of trapped matter|
Herein is described a process method and device used for nonporous, or porous media, that is metallic, ceramic, or of rock based compositions, such as geologic materials which may house inclusions such that under electromigration, thermophoresis, electrophoresis, magnetophoresis, electromagnetics, leads to combined advection, convection, electro-magnetic kinetics, osmosis, and diffusion. Meaning that under the influence of a solvent, cell, enclosure, contacts, and second enclosure material, yields the expulsion of trapped housed matter such as kerogen, oil, gas condensates, water-oil mixtures, hydrocarbons, terpenes, organic compounds, methane, inorganic material, solvent, or other organic material(s), or oil-gas-water type natural resource material.
|Microchannel gel electrophoretic separation systems and methods for preparing and using|
A micro-analytical platform for performing electrophoresis-based immunoassays was developed by integrating photopolymerized cross-linked polyacrylamide gels within a microfluidic device. The microfluidic immunoassays are performed by gel electrophoretic separation and quantifying analyte concentration based upon conventional polyacrylamide gel electrophoresis (page).
|Methods of analyzing plaque|
The invention provides a method of measuring ammonia and/or calcium in a sample of dental plaque, comprising obtaining the sample of plaque and measuring ammonium and calcium ions using capillary electrophoresis, together with methods of diagnosis, treatment and screening based on evaluation of plaque.. .
|Composition and method for gel electrophoresis with in-situ calibration|
The invention relates to, among other things, a method for performing electrophoresis with in-situ calibration. The method includes combining a volume of a test sample with a volume or quantity of a calibrating sample to form a final volume, where the volume of the calibrating sample includes a known concentration of a calibrator and the final volume includes a known ratio of test sample to calibrating sample.
|Leakage current sense circuit for error detection in an improved capillary electrophoresis-electrospray ionization- mass spectrometry system|
Aspects of the present innovations relate to improved systems that may perform capillary electrophoresis (ce) and ce in conjunction with electrospray ionization (esi) as an input to a mass spectrometry system (ms). Embodiments may use a current sense circuit at a high voltage output from an ms-esi power supply in conjunction with additional elements to identify fault conditions associated with leakage current, to confirm the continuity of ce connections, and to provide improved system protection..
|Capillary electrophoresis method for fine structural analysis of enoxaparin sodium|
A capillary electrophoresis method for quantitatively analyzing characteristic oligosaccharide present in enoxaparin sodium is provided in this invention. The method may be used for quantitatively determining the contents of disaccharides, trisaccharides, tetrasaccharides and in particular oligosaccharides having a 1,6-anhydro ring, which are unique compounds for enoxaparin sodium, within an exhaustively digested enoxaparin sodium sample with a mixture of heparinase i, ii, and iii, so as to quantitatively determine the molar percentage of oligosaccharides having 1,6-anhydro ring in enoxaparin sodium.
A high-resolution biosensor for analysis of biomolecules is provided. The high-resolution biosensor comprises a functional unit comprising a conducting material with an atomic-scale thickness and a micro-nano fluidic system unit.
|Gelc-ms using stain free technology|
Disclosed herein is a method of preparing a protein sample for mass spectroscopy. The method includes separating proteins of the sample on an electrophoresis gel; contacting the proteins with a halo-substituted organic compound; exposing the gel to uv light; detecting fluorescence emitted from the electrophoresis gel; excising at least one portion of the electrophoresis gel based upon the detected fluorescence, wherein said at least one portion contains proteins of the protein sample; and subjecting proteins from the at least one portion to mass spectroscopy.
|Three dimensional microelectrode system for dielectrophoresis|
A dielectrophoresis apparatus for separating particles from a sample, including an apparatus body; a dielectrophoresis channel in the apparatus body, the dielectrophoresis channel having a central axis, a bottom, a top, a first side, and a second side; a first mesa projecting into the dielectrophoresis channel from the bottom and extending from the first side across the dielectrophoresis channel to the second side, the first mesa extending at an angle to the central axis of the dielectrophoresis channel; a first electrode extending along the first mesa; a second mesa projecting into the dielectrophoresis channel from the bottom and extending from the first side across the dielectrophoresis channel to the second side, the second mesa extending at an angle to the central axis of the dielectrophoresis channel; a space between at least one of the first electrode and the second side or the second electrode and the second side; and a gap between the first electrode and the second electrode.. .
|Electrophoresis apparatus, capillary array, and capillary unit|
The apparatus has a configuration provided with a plurality of capillary units each of which can be attached/detached to/from the apparatus, and performs analysis for capillaries after sealing of a polymer by attaching the capillaries by the number in accordance with the number of samples. Since analysis can be performed by using capillaries by the number identical with that of the samples to be analyzed, wasteful polymer is not used in the capillaries not used for the analysis.
|Capillary electrophoresis system|
The invention is an improved multiplex capillary electrophoresis instrument or module with at least four and preferably six user-accessible vertically stacked drawers. An x-z stage moves samples from the user accessible drawers to the capillary array for analysis.
|Reversible current gel electrophoresis device for separating biological macromolecules|
Cassette bodies for use with electrophoresis apparatus can be formed of a single piece of molded or machined plastic. Such cassette bodies can include a plurality of channels that pass through the cassette body, from a proximal end to a distal end.
|Traveling wave dielectrophoretic displays|
A traveling wave dielectrophoresis display includes a display cell and a plurality of first particles contained within the display cell, the plurality of first particles having a first color. A plurality of electrodes in proximity to the display cell and generate a traveling wave dielectrophoresis field which distributes the plurality of first particles within the display cell to alter its optical characteristics..
|Base for electrophoresis display and method of manufacturing the same, and electrophoresis display and method of manufacturing the same|
A base for an electrophoresis display includes: a base; partition walls that are provided on one surface of the base, the opposite side to the one surface being opened; an electrophoresis material liquid that includes a dispersion medium filling at least partial cells among a plurality of cells on the base partitioned by partition walls and electrophoresis particles; and a membrane filter that is provided to close openings of the partition walls and has pores through which the dispersion medium is able to pass and the electrophoresis particles are unable to pass.. .
|Electrophoresis particle, method of manufacturing electrophoresis particle, electrophoresis dispersion liquid, electrophoresis sheet, electrophoresis device and electronic apparatus|
An electrophoresis particle of the embodiment includes a mother particle and a covering layer which covers at least a part of the mother particle, wherein the covering layer includes a shell which is consisted of an organic polymer and which cellulary engulfs the mother particle and a polymer which is bonded on the surface of the shell and the polymer is one that a monomer has been polymerized using living radical polymerization, setting the polymerization initiating group as the starting point.. .
|Methods for separation and immuno-detection of biomolecules, and apparatus related thereto|
Disclosed are methods and apparatus for separation of biomolecules via two-dimensional gel electrophoresis, methods and apparatus for immunoblotting separated biomolecules, and methods for the use of biomolecules processed via the methods and apparatus of the present invention, including use in a clinical setting. The methods and apparatus for separation of biomolecules via two-dimensional gel comprises vertical agarose gel electrophoresis in the first dimension, and the electrophoresis of a novel non-denaturing 3-35% concave gradient polyacrylamide gel in the second dimension.
|Microfluidic interface for a microchip|
A capillary electrophoresis system which provides a microfluidic chip for capillary electrophoresis and a microfluidic interface module which fluidicly couples the microfluidic chip to external fluid sources and or external repositories.. .
|Method for isotopic measurement by icpms|
C) in the continuity of the preceding step, performing an isotope measurement of the species detected in the form of a substantially constant amplitude signal by using an inductively coupled plasma mass spectrometer (icpms) connected by direct coupling with the capillary electrophoresis device.. .
|Multichannel preparative electrophoresis system|
The invention provides an electrophoresis cassette, methods for making the electrophoresis cassette, and method of fractionating analytes from a sample based upon electrophoretic mobility in a single application of the sample to an electrophoretic system.. .